System and method for sensing and trapping nanoparticles with plasmonic nanopores
US-2017284935-A1 · Oct 5, 2017 · US
US9921174B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9921174-B2 |
| Application number | US-201615275984-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 26, 2016 |
| Priority date | Nov 6, 2012 |
| Publication date | Mar 20, 2018 |
| Grant date | Mar 20, 2018 |
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Systems and methods for controlling the temperature of small volumes such as yoctoliter volumes, are described. The systems include one or more plasmonic nanostructures attached at or near a nanopore. Upon excitation of the plasmonic nanostructures, such as for example by exposure to laser light, the nanoparticles are rapidly heated thereby causing a change in the ionic conductance along the nanopore. The temperature change is determined from the ionic conductance. These temperature changes can be used to control rapid thermodynamic changes in molecular analytes as they interact with the nanopore.
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What is claimed is: 1. A method for analyzing polymers comprising: providing plasmonic nanostructures; providing a surface containing a nanopore; affixing the plasmonic nanostructures proximate the nanopore; disposing a polymer to be analyzed in the nanopore; emitting light of sufficient intensity and wavelength to excite the plasmonic nanostructures and induce a change in temperature within the nanopore; analyzing the polymer disposed in the nanopore by use of the change in temperature within the nanopore. 2. The method of claim 1 wherein the analyzing includes assessing at least one of (i) physical changes to polymers, (ii) chemical changes to polymers, (iii) thermodynamic properties of polymers, and (iv) kinetic properties of polymers. 3. The method of claim 1 wherein during the emitting of the light, the light is absorbed at or near the surface plasmon resonance and increases the temperature of the nanostructures. 4. The method of claim 1 wherein the analyzing includes estimating at least one of (i) absorbance of emitted light by nanostructures, (ii) excitation of surface plasmons in nanostructures due to absorption of light, (iii) change in temperature of nanostructures due to excitation of surface plasmons by light, and (iv) estimation of the change in temperature in the vicinity of the nanostructure, including at the nanopore and polymers. 5. The method of claim 1 wherein the providing a surface containing a nanopore includes providing a substrate including a biological layer that defines the nanopore. 6. The method of claim 5 wherein the providing plasmonic nanostructures includes providing one or more metallic nanoparticles tethered to a surface of the biological layer. 7. The method of claim 6 wherein the metallic nanoparticles have a size within a range of from about 10 nm to about 1,000 nm. 8. The method of claim 6 wherein the metallic nanoparticles are tethered to the biological layer by at least one oligomer. 9. The method of claim 8 wherein the oligomer is an oligonucleotide having from 10 to 500 repeating units. 10. The method of claim 5 wherein the affixing the plasmonic nanostructures proximate the nanopore is performed by tethering metallic nanoparticles to the biological layer by at least one oligomer. 11. The method of claim 10 wherein the oligomer is an oligonucleotide having from 10 to 500 repeating units. 12. The method of claim 1 wherein the emitted light is selected from the group consisting of a laser, an incandescent light source, a light emitting diode, and an arc lamp. 13. The method of claim 1 wherein the plasmonic nanostructures include metallic nanoparticles. 14. The method of claim 13 wherein the metallic nanoparticles have a size within a range of from about 10 nm to about 1,000 nm. 15. The method of claim 1 wherein the plasmonic nanostructures include metallic nanoparticles and the nanopore is defined in a biological layer, wherein affixing is performed by attaching the metallic nanoparticles to the biological layer using at least one oligomer.
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